ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0459 NCALD SNP Missense_Mutation 8 102701563 C T 31 100 MEL MEL-JWCI-WGS-29 NCALD SNP Silent 8 102731486 G A 37 50 MM MM-0529 NCALD SNP Missense_Mutation 8 102731714 A C 13 79 PRAD PR-3023 NCALD SNP Missense_Mutation 8 102705043 G A 39 83 LUAD TCGA-05-4396 NCALD SNP Missense_Mutation 8 102731650 G T 39 100 LUAD TCGA-05-4410 NCALD SNP Missense_Mutation 8 102705114 T C 56 91 LUSC TCGA-18-3409 NCALD SNP Missense_Mutation 8 102701575 G A 35 88 GBM TCGA-19-2629 NCALD SNP Silent 8 102705056 T C 55 51 LUAD TCGA-64-5775 NCALD SNP Silent 8 102731843 G A 48 86 CRC TCGA-AA-3977 NCALD SNP Silent 8 102705047 G T 33 60 CRC TCGA-AA-A00N NCALD SNP Silent 8 102701564 G A 38 47 UCEC TCGA-B5-A11E NCALD SNP Missense_Mutation 8 102701581 C T 17 100 HNSC TCGA-BA-5152 NCALD SNP Silent 8 102701558 C T 31 52 HNSC TCGA-CR-6481 NCALD SNP Missense_Mutation 8 102731491 C G 32 99 HNSC TCGA-CV-5439 NCALD SNP Missense_Mutation 8 102731518 C A 21 99 UCEC TCGA-D1-A17Q NCALD SNP Missense_Mutation 8 102701563 C T 31 100